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ADAMTS13 and epilepsy are reported together in 1 article.
Gene
ADAMTS13
- HGNC
- HGNC:1366
8articles
8mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
Phenotype
Epilepsy
- HPO
- HP:0001250
2,084articles
2,084mentions
12co-reported genes shown
Most co-reported genes (articles)
Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.
Publications
1 records shown · first 60Thrombotic thrombocytopenic purpura in a patient with systemic lupus erythematosus after anifrolumab: a possible association.
PMID 41561490 | PMCID PMC12814899 | DOI 10.22551/2025.49.1204.10330 · Archive of clinical cases · 2025 · 3 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | ADAMTS13 | “Laboratory evaluation demonstrated microangiopathic hemolytic anemia, severe thrombocytopenia, elevated lactate dehydrogenase, and markedly reduced ADAMTS13 activity (10%).” | 0.98 | hgnc_dict_v1 |
| phenotype | epilepsy | “A 32-year-old woman with long-standing SLE developed fever, mucocutaneous bleeding, confusion, and seizures approximately ten weeks after initiating anifrolumab.” | 0.93 | phenotype_alias_lexicon_v2 |
| phenotype | systemic lupus erythematosus | “Thrombotic thrombocytopenic purpura in a patient with systemic lupus erythematosus after anifrolumab: a possible association.” | 0.98 | phenotype_alias_lexicon_v2 |